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- ΔF508 abstract "ΔF508 (delta-F508, full name CFTRΔF508 or F508del-CFTR; rs113993960) is a specific mutation within the gene for a protein called the cystic fibrosis transmembrane conductance regulator (CFTR). The mutation is a deletion of the three nucleotides that comprise the codon for phenylalanine (F) at position 508. A person with the CFTRΔF508 mutation will produce an abnormal CFTR protein that lacks this phenylalanine residue. This protein does not escape the endoplasmic reticulum for further processing. Having two copies of this mutation (one inherited from each parent) is the leading cause of cystic fibrosis (CF).".
- ΔF508 wikiPageExternalLink snp_ref.cgi?rs=113993960.
- ΔF508 wikiPageExternalLink subtypes.htm.
- ΔF508 wikiPageID "2447734".
- ΔF508 wikiPageLength "9941".
- ΔF508 wikiPageOutDegree "38".
- ΔF508 wikiPageRevisionID "707207147".
- ΔF508 wikiPageWikiLink Amino_acid.
- ΔF508 wikiPageWikiLink Base_pair.
- ΔF508 wikiPageWikiLink Category:Cystic_fibrosis.
- ΔF508 wikiPageWikiLink Category:Mutation.
- ΔF508 wikiPageWikiLink Caucasian_race.
- ΔF508 wikiPageWikiLink Chloride.
- ΔF508 wikiPageWikiLink Cholera.
- ΔF508 wikiPageWikiLink Congenital_absence_of_the_vas_deferens.
- ΔF508 wikiPageWikiLink Cystic_fibrosis.
- ΔF508 wikiPageWikiLink Cystic_fibrosis_transmembrane_conductance_regulator.
- ΔF508 wikiPageWikiLink DNA.
- ΔF508 wikiPageWikiLink Dehydration.
- ΔF508 wikiPageWikiLink Delta_(letter).
- ΔF508 wikiPageWikiLink Diarrhea.
- ΔF508 wikiPageWikiLink Endoplasmic_reticulum.
- ΔF508 wikiPageWikiLink Europe.
- ΔF508 wikiPageWikiLink Gene.
- ΔF508 wikiPageWikiLink Genetic_carrier.
- ΔF508 wikiPageWikiLink Genetic_code.
- ΔF508 wikiPageWikiLink Heterozygote_advantage.
- ΔF508 wikiPageWikiLink Isoleucine.
- ΔF508 wikiPageWikiLink Mendelian_inheritance.
- ΔF508 wikiPageWikiLink Mucous_membrane.
- ΔF508 wikiPageWikiLink Mutation.
- ΔF508 wikiPageWikiLink Nucleotide.
- ΔF508 wikiPageWikiLink Osmosis.
- ΔF508 wikiPageWikiLink Phenylalanine.
- ΔF508 wikiPageWikiLink Protein.
- ΔF508 wikiPageWikiLink Tuberculosis.
- ΔF508 wikiPageWikiLink Typhoid_fever.
- ΔF508 wikiPageWikiLink Vas_deferens.
- ΔF508 wikiPageWikiLink Vibrio_cholerae.
- ΔF508 wikiPageWikiLink Zygosity.
- ΔF508 wikiPageWikiLinkText "F508del".
- ΔF508 wikiPageWikiLinkText "ΔF508".
- ΔF508 wikiPageWikiLinkText "ΔF508-CFTR".
- ΔF508 wikiPageUsesTemplate Template:Refimprove.
- ΔF508 wikiPageUsesTemplate Template:Reflist.
- ΔF508 subject Category:Cystic_fibrosis.
- ΔF508 subject Category:Mutation.
- ΔF508 hypernym Mutation.
- ΔF508 type Bird.
- ΔF508 type Diacritic.
- ΔF508 type Disorder.
- ΔF508 type Pediatric.
- ΔF508 type Redirect.
- ΔF508 comment "ΔF508 (delta-F508, full name CFTRΔF508 or F508del-CFTR; rs113993960) is a specific mutation within the gene for a protein called the cystic fibrosis transmembrane conductance regulator (CFTR). The mutation is a deletion of the three nucleotides that comprise the codon for phenylalanine (F) at position 508. A person with the CFTRΔF508 mutation will produce an abnormal CFTR protein that lacks this phenylalanine residue.".
- ΔF508 label "ΔF508".
- ΔF508 sameAs Q423990.
- ΔF508 sameAs ΔF508.
- ΔF508 sameAs ΔF508.
- ΔF508 sameAs m.07ds4v.
- ΔF508 sameAs Q423990.
- ΔF508 wasDerivedFrom ΔF508?oldid=707207147.
- ΔF508 isPrimaryTopicOf ΔF508.